A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976949



Internal ID18612155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:72445519..72451513hg38UCSC Ensembl
Innerchr15:72737860..72743854hg19UCSC Ensembl
Innerchr15:70524914..70530908hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg385995
hg195995
hg185995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2030035, nssv2030029, nssv2030036, nssv2030033, nssv2030030, nssv2030032, nssv2030027, nssv2030028, nssv2030034, nssv2030031
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976949
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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